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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530232Generated: November 2, 2026

Acetic Anhydride → 1,6-Octadien-1-ol, 3,7-dimethyl-, 1-acetate, (3S)-

https://huagongshe.com/reaction/530232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant(S)-(-)-CitronellalHCID 443157—
ReactantPotassium AcetateHCID 517044—
SolventWaterHCID 962—
Product1,6-Octadien-1-ol, 3,7-dimethyl-, 1-acetate, (3S)-HCID 86718786—

Reaction Conditions

Temperature120 °C

Reaction Steps

A 50 mL round-bottom-flask equipped with a condenser was charged with acetic anhydride (6.1 mL, 64.8 mmol), potassium acetate (0.51 g, 5.18 mmol) and triethylamine (4.5 mL, 32.4 mmol). To the stirred mixture was (S)-3,7-dimethyloct-6-enal (5.0 g, 32.4 mmol) slowly. The reaction mixture was heated to 120° C. for 7.5 hours. After cooling to room temperature, the reaction mixture was poured into water (25 mL) and then extracted with toluene (10 mL). The organic layer was washed with saturated aqueous sodium carbonate (25 mL×2) and brine (25 mL). The material was transferred to a 50 ml round-bottom-flask and the separatory funnel was washed with toluene (1 mL). The solution of the title compound in toluene (11 ml) (15.7 g) was used directly for the next step. Mass spectrum (ESI +ve) m/z 187 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353063B2
Source datasetuspto-grants-2016_05
ORD IDord-4ab4bdfa095143c3b27f6b6df3a44c3e
Source noteuspto-grants-2016_05